Synfacts 2006(8): 0834-0834  
DOI: 10.1055/s-2006-942006
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart · New York

Enantioselective Catalytic Addition of Phenylacetylene to Aromatic Ketones

Contributor(s): Paul Knochel, Andrei Gavryushin
C. Chen, L. Hong, Z.-Q. Xu, L. Liu, R. Wang*
Lanzhou University and Lanzhou Institute of Chemical Physics, P. R. of China
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Publikationsverlauf

Publikationsdatum:
21. Juli 2006 (online)

Significance

Catalytic asymmetric propargyl­ation of carbonyl compounds has received much attention recently due to the high importance of the resulting chiral propargylic alcohols as synthetic intermediates. Ketones are usually not easy substrates for this reaction, therefore, the development of new methods for their enantioselective propargylation is a challenging task. The authors developed here a new procedure, affording a highly enantioselective addition of phenylacetylene to acetophenones even by using very low amounts of catalyst. The chiral ligand can be prepared from chiral phenylglycine in three steps.